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布鲁氏菌外膜蛋白基因omp19序列克隆与原核表达

Sequence Cloning and Prokaryotic Expression of omp19 Outer Membrane Protein Gene in Brucella
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摘要 目的:研究猪型布鲁氏菌外膜蛋白基因omp19的序列性质,同时,进行目的基因的原核表达。方法:以猪型布鲁氏菌基因组作为模板进行基因序列的扩增,利用大肠杆菌原核表达系统进行重组表达。结果:猪型布鲁氏菌外膜蛋白基因omp19的开放阅读框序列全长为534 bp,演绎177个氨基酸。诱导表达的重组蛋白质的理论分子量为17.6 kD,而且实际大小与理论值一致。结论:成功表达了Omp19分子,为进一步研究Omp19分子的免疫保护作用奠定了基础。 Objective: The sequence properties of swine Brucella ompl9 gene were studied,and this gene was expressed at the same time, using E. coli prokaryotie expression system. Method: Swine Brucella genome was taken as the template for gene sequence amplification, and ompl9 gene was recombinantly expressed using E. coli prokaryotic expression system. Result: The ORF sequence of ompl9 gene in- cluded 534 bp, and it could encoded 177 amino acids. The molecular weight of this recombinant molecule Ompl9 was 17. 6 kD, and it was consistent with the theoretical value. Conclusion: The Ompl9 molecule was successfully expressed, and these work laid foundation for thefurther study on immune protective function of Ompl9.
出处 《生物技术》 CAS CSCD 北大核心 2013年第6期8-10,共3页 Biotechnology
关键词 猪型布鲁氏菌 外膜蛋白质 omp19基因 序列克隆 原核表达 Swine Brucella Outer membrane protein ompl9 gene Sequence cloning Prokaryotic expression
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